The role of the iminosugar N-butyldeoxynojirimycin (miglustat) in the management of type I (non-neuronopathic) Gaucher disease: a position statement (Q28182540)

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scientific article (publication date: 2003)

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English	The role of the iminosugar N-butyldeoxynojirimycin (miglustat) in the management of type I (non-neuronopathic) Gaucher disease: a position statement	scientific article (publication date: 2003)

Statements

scholarly article

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20 December 2019

1 reference

Europe PubMed Central

The role of the iminosugar N-butyldeoxynojirimycin (miglustat) in the management of type I (non-neuronopathic) Gaucher disease: a position statement (English)

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Europe PubMed Central

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20 December 2019

Gaucher's disease

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based on heuristic

inferred from title

2

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Europe PubMed Central

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20 December 2019

Martin Hrebicek

14

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20 December 2019

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T M Cox

1

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20 December 2019

G Andria

3

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20 December 2019

M Beck

4

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20 December 2019

N Belmatoug

5

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20 December 2019

B Bembi

6

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20 December 2019

R Chertkoff

7

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20 December 2019

S Vom Dahl

8

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20 December 2019

D Elstein

9

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20 December 2019

A Erikson

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20 December 2019

M Giralt

11

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20 December 2019

R Heitner

12

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20 December 2019

C Hollak

13

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20 December 2019

S Lewis

15

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20 December 2019

A Mehta

16

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20 December 2019

G M Pastores

17

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20 December 2019

A Rolfs

18

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20 December 2019

M C Sa Miranda

19

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20 December 2019

A Zimran

20

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20 December 2019

Advisory Council to the European Working Group on Gaucher Disease

21

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20 December 2019

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publication date

1 January 2003

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20 December 2019

Journal of Inherited Metabolic Disease

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20 December 2019

26

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20 December 2019

6

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20 December 2019

513-526

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20 December 2019

3 Gaucher's disease: clinical features and natural history

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https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

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The health-related quality of life of adults with Gaucher's disease receiving enzyme replacement therapy: results from a retrospective study

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

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Substrate reduction therapy for glycosphingolipid storage disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

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Novel oral treatment of Gaucher's disease with N-butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

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The natural course of Gaucher disease in The Netherlands: implications for monitoring of disease manifestations

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

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Quality of life assessment in adults with type 1 Gaucher disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

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High prevalence of low serum vitamin B12 in a multi-ethnic Israeli population

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

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Withdrawal of enzyme replacement therapy in Gaucher's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

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Partial enzyme deficiencies: residual activities and the development of neurological disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

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N-butyldeoxynojirimycin is a novel inhibitor of glycolipid biosynthesis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

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METABOLISM OF GLUCOCEREBROSIDES. II. EVIDENCE OF AN ENZYMATIC DEFICIENCY IN GAUCHER'S DISEASE.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

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The tolerability and pharmacokinetics of N-butyl-deoxynojirimycin in patients with advanced HIV disease (ACTG 100). The AIDS Clinical Trials Group (ACTG) of the National Institute of Allergy and Infectious Diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

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Replacement therapy for inherited enzyme deficiency--macrophage-targeted glucocerebrosidase for Gaucher's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

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Glucocerebrosidase genotype of Gaucher patients in The Netherlands: limitations in prognostic value

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of low-dose enzyme replacement therapy on bones in Gaucher disease patients with severe skeletal involvement

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

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inferred from PubMed ID database lookup

Dixon quantitative chemical shift imaging is a sensitive tool for the evaluation of bone marrow responses to individualized doses of enzyme supplementation therapy in type 1 Gaucher disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

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The safety and efficacy of combination N-butyl-deoxynojirimycin (SC-48334) and zidovudine in patients with HIV-1 infection and 200-500 CD4 cells/mm3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gaucher's disease: genetic counselling and population screening.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Antibody response in patients with Gaucher disease after repeated infusion with macrophage-targeted glucocerebrosidase

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

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Gaucher disease. Clinical, laboratory, radiologic, and genetic features of 53 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical monitoring after cessation of enzyme replacement therapy in M. Gaucher

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzyme replacement therapy for Gaucher disease: skeletal responses to macrophage-targeted glucocerebrosidase

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation analysis of the acid beta-glucosidase gene in a patient with type 3 Gaucher disease and neutralizing antibody to alglucerase

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

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Prevalence of lysosomal storage disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

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Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: a report from the Gaucher Registry

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

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inferred from PubMed ID database lookup

Preparation of the active isomer of 1-phenyl-2-decanoylamino-3-morpholino-1-propanol, inhibitor of murine glucocerebroside synthetase

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

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Replacement therapy with imiglucerase for type 1 Gaucher's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

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Enzyme therapy in type 1 Gaucher disease: comparative efficacy of mannose-terminated glucocerebrosidase from natural and recombinant sources

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Management of neuronopathic Gaucher disease: a European consensus.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

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Low-dose enzyme replacement therapy for Gaucher's disease: effects of age, sex, genotype, and clinical features on response to treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical course of treated and untreated Gaucher disease. A study of 45 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correlation of bone marrow response with hematological, biochemical, and visceral responses to enzyme replacement therapy of nonneuronopathic (type 1) Gaucher disease in 30 adult patients.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Individualised low-dose alglucerase therapy for type 1 Gaucher's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interruption in enzyme replacement therapy for Gaucher disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma and metabolic abnormalities in Gaucher's disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

2 Gaucher's disease: molecular, genetic and enzymological aspects

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzyme therapy in Gaucher disease type 1: dosage efficacy and adverse effects in 33 patients treated for 6 to 24 months

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Failure of alglucerase infused into Gaucher disease patients to localize in marrow macrophages.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the Spanish Gaucher's disease registry: clinical and genetic characteristics.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

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Glucocerebrosidase (Gaucher disease).

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

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inferred from PubMed ID database lookup

Low-dose N-butyldeoxynojirimycin (OGT 918) for type I Gaucher disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14605497

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/A:1025902113005

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Consolidated OpenCitations Corpus – April 2017

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20 December 2019

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Consolidated OpenCitations Corpus – April 2017

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2 references

Consolidated OpenCitations Corpus – April 2017

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Europe PubMed Central

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20 December 2019

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